Early In-Hospital ARNI After MI: Promising but PARADISE-MI Anchors Caution
This meta-analysis pools 12 RCTs of early in-hospital sacubitril/valsartan versus ACEI/ARB in post-MI patients with LVEF below 50%, quantifying a MACE and ventricular arrhythmia signal that is heavily dependent on small, unblinded trials.
Early ARNI therapy post-AMI cuts cardiovascular events by 42%.
Heart failure is a common complication after acute myocardial infarction (AMI) in patients with impaired left ventricular ejection fraction (LVEF). Early angiotensin-receptor-neprilysin inhibitor (ARNI) initiation reduced major adverse cardiovascular events (MACEs) by 42% and improved LVEF by 2.54%, but increased symptomatic hypotension risk. ARNI therapy shows promise for early post-AMI management, but the increased risk of hypotension requires careful monitoring. Early ARNI initiation post-AMI reduces MACEs and improves LVEF but watch for hypotension.
📊 Deep Analysis Available
Subscribers get the full breakdown: study design, outcomes, pharmacist implications, clinical pearls, GRADE evidence grade, and a downloadable PDF report.
Authors:Nguyen Q, Tran TTQ, Liao CT, Hung CL, Chang HY, Chen CW, Lin YC, Huang CY, Hsu CY
Citation:Nguyen Q, Tran TTQ, Liao CT, et al. Early in-hospital initiation of angiotensin-receptor-neprilysin inhibitor in post-acute myocardial infarction patients with impaired left ventricular systolic function: a systematic review and meta-analysis of randomized controlled trials. Frontiers in cardiovascular medicine. 2026;13:1877075. doi:10.3389/fcvm.2026.1877075
Subscribers receive access to a complete clinical analysis, available online and as a downloadable PDF.
Executive Summary
Study Design
Patient Population
Primary Outcomes
Secondary Outcomes & Safety Profile
Pharmacist Implications
Clinical Pearls
Limitations
Controversies & Evidence Gaps
Cost & Logistics
Want the full analysis?
Subscribe to PharmD Signal for unrestricted access to every deep analysis, plus PDF reports, GRADE evidence grades, and pharmacist implications for every article we publish.